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Organization name
UDI-DI code
Reference / catalog number

PZN 7470157 — Class I MDR by PakuMed medical…

MD Atlas
PakuMed medical products GmbH

EUDAMED last updated this device on May 27, 2026

PZN 7470157

426014678ANOKRYOJE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PakuMed medical products GmbH
UDI-DI code: 04260146783014
Reference / catalog number: PZN 7470157

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View device family (Basic UDI)

Manufacturer information

Organization name: PakuMed medical products GmbH
SRN: DE-MF-000005123
Manufacturer status: Active

Related devices

PZN 3941536426014678ANOKRYOJEOn the market PZN 19075087426014678ANOKRYOJEOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260146783014
Basic UDI-DI: 426014678ANOKRYOJE
Reference / catalog number: PZN 7470157
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The ANOKRYO lubricant serves as an aid to the ANOKRYO cold stick and dilator to facilitate anal insertion in cases of haemorrhoids, anal fissures and other anal complications.
Additional information URL: https://pakumed.de/wp-content/uploads/2022/07/IIc-Gebrauchsanweisung_IFU_-Deutsch_Englisch_-Arabisch_Rev.4.pdf
Clinical sizes: 2 pieces of 30 g each

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04260146783014

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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